HCID 9946422, compound → HCID 18460631, compound
Reaction equation
[CH2:1]([N:3]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=2[N:5]=[C:4]1[NH:12][CH2:13][CH2:14][N:15]1[CH2:20][CH2:19][N:18]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][N:22]=2)[CH2:17][CH2:16]1)[CH3:2].[BrH:27].N1C=CC=CC=1N1CCN(CCNC2N(C(C)C)C3C=CC=CC=3N=2)CC1>>[BrH:27].[N:22]1[CH:23]=[CH:24][CH:25]=[CH:26][C:21]=1[N:18]1[CH2:17][CH2:16][N:15]([CH2:14][CH2:13][NH:12][C:4]2[N:3]([CH2:1][CH3:2])[C:7]3[CH:8]=[CH:9][CH:10]=[CH:11][C:6]=3[N:5]=2)[CH2:20][CH2:19]1Participants
3
Procedure
[(1-ethylbenzimidazol-2-yl) [2-(4-(2-pyridyl)piperazinyl)ethyl]amine] (Compound 41). p (kk) 1-(Pyridin-2-yl)-4-(2-[1-isopropylbenzimidazol-2-yl]aminoethyl)piperazine hydrobromide (Compound 42).
Sources & evidence
- ORD record
- ord-c65e1dd429b44be6b6574135289ffd69
- Source dataset
- uspto-grants-2001_09
- Patent number
- US06284759B1
Reaction notes
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